Benicar
- Product NDC
- 50090-0877
- 11-digit product format
- 500900877
- Labeler code
- 50090
- Product ID
- 50090-0877_01dc0513-a4bf-420f-8908-d9a3e1bc3580
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- olmesartan medoxomil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA021286
- Marketing category
- NDA
- Marketing start
- 2002-04-25
- Marketing end
- 0000-00-00
- Substance
- OLMESARTAN MEDOXOMIL
- Active strength
- 20 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-0877-0 | 50090087700 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-0877-0) | 2014-11-28 | 0000-00-00 | No | No | Current |